Global MSAT Senior/Principal DP Product Steward

Roche

Senior/Principal Product Steward managing technical health of commercial large molecule products at Roche. Driving technical industrialization and overseeing product development from launch to divestment.

Posted 7/20/2026full-timeBasel • 🇨🇭 SwitzerlandSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Drug Product Manufacturing, Technical Oversight, and Process Development, with a strong focus on regulatory compliance and patient-centric design. Proven ability to lead cross-functional teams and drive technical industrialization strategies for biological molecules.

Highest-signal resume keywords

Drug Product ManufacturingTechnical OversightProcess DevelopmentRegulatory SubmissionCross-Functional Leadership

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Technical IndustrializationRisk ManagementManufacturabilityPerformance ManagementTechnology TransferProcess Validation

Soft Skills

Stakeholder InteractionProblem Solving

Certifications & Qualifications

B.S. or M.S. Degree in Scientific Discipline

Industry Keywords

BiotechnologyPharmacyBiological MoleculesPatient-CentricityHealth Authority Requirements

About the role

Key responsibilities & impact

Driving seamless technical industrialization and sustaining and improving the technical health of commercial products
Developing technical strategic roadmap
Owning & mitigating technical risks
Providing technical oversight of commercial DPs from launch to divestment to consistently deliver quality products to patients
Identifying, defining, and delivering DP-related technical industrialization strategies and technical improvements to ensure successful launch
Driving technical product health including strategic roadmap, risk management, manufacturability and performance management
Serving as a primary product technical owner for site leadership and quality functions when investigating product or process issues across the commercial lifecycle
Representing the product in key technical governance forums and senior stakeholder interactions

Requirements

What you’ll need

B.S. or M.S. degree in a scientific discipline (biotechnology, pharmacy, biology etc.)
7+/10+ years of relevant industrial experience in platform specific process development or in supporting platform specific manufacturing operations (e.g. DS Bio, DP SM etc.)
Proven record in Drug Product manufacturing and product and technology industrialization as well as process development in the field of biological molecules
Significant cross-functional matrix leadership experience
Demonstrated experience with technology transfer and/or with process validation
Strong understanding of regulatory submission and health authority requirements as well as patient needs / patient-centricity as key elements of design and delivery

Benefits

Comp & perks

Open dialogue
Genuine connections
Personal expression